LU93078I2 - COMBIMETINIB, POSSIBLY IN ANY FORM PROTECTED BY THE BASIC PATENT, INCLUDING PHARMACEUTICALLY ACCEPTABLE SALTS AND SOLVATES, IN PARTICULAR COBIMETINIB HEMIFUMARATE - Google Patents

COMBIMETINIB, POSSIBLY IN ANY FORM PROTECTED BY THE BASIC PATENT, INCLUDING PHARMACEUTICALLY ACCEPTABLE SALTS AND SOLVATES, IN PARTICULAR COBIMETINIB HEMIFUMARATE Download PDF

Info

Publication number
LU93078I2
LU93078I2 LU93078C LU93078C LU93078I2 LU 93078 I2 LU93078 I2 LU 93078I2 LU 93078 C LU93078 C LU 93078C LU 93078 C LU93078 C LU 93078C LU 93078 I2 LU93078 I2 LU 93078I2
Authority
LU
Luxembourg
Prior art keywords
solvates
pharmaceutically acceptable
acceptable salts
combimetinib
possibly
Prior art date
Application number
LU93078C
Other languages
French (fr)
Original Assignee
Exelixis Inc
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Family has litigation
First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=37728416&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=LU93078(I2) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Application filed by Exelixis Inc filed Critical Exelixis Inc
Publication of LU93078I2 publication Critical patent/LU93078I2/en

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D205/00Heterocyclic compounds containing four-membered rings with one nitrogen atom as the only ring hetero atom
    • C07D205/02Heterocyclic compounds containing four-membered rings with one nitrogen atom as the only ring hetero atom not condensed with other rings
    • C07D205/04Heterocyclic compounds containing four-membered rings with one nitrogen atom as the only ring hetero atom not condensed with other rings having no double bonds between ring members or between ring members and non-ring members
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/397Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having four-membered rings, e.g. azetidine
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P17/00Drugs for dermatological disorders
    • A61P17/02Drugs for dermatological disorders for treating wounds, ulcers, burns, scars, keloids, or the like
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P17/00Drugs for dermatological disorders
    • A61P17/06Antipsoriatics
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00Antineoplastic agents
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00Antineoplastic agents
    • A61P35/02Antineoplastic agents specific for leukemia
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P43/00Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D205/00Heterocyclic compounds containing four-membered rings with one nitrogen atom as the only ring hetero atom
    • C07D205/02Heterocyclic compounds containing four-membered rings with one nitrogen atom as the only ring hetero atom not condensed with other rings
    • C07D205/06Heterocyclic compounds containing four-membered rings with one nitrogen atom as the only ring hetero atom not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D401/00Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
    • C07D401/02Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
    • C07D401/04Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings directly linked by a ring-member-to-ring-member bond
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D401/00Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
    • C07D401/02Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
    • C07D401/06Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a carbon chain containing only aliphatic carbon atoms
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D401/00Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
    • C07D401/02Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
    • C07D401/12Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a chain containing hetero atoms as chain links
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D401/00Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
    • C07D401/14Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing three or more hetero rings
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D403/00Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
    • C07D403/02Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
    • C07D403/04Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings directly linked by a ring-member-to-ring-member bond
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D403/00Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
    • C07D403/02Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
    • C07D403/06Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings linked by a carbon chain containing only aliphatic carbon atoms
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D403/00Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
    • C07D403/02Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
    • C07D403/12Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D405/00Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
    • C07D405/02Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings
    • C07D405/12Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings linked by a chain containing hetero atoms as chain links
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D409/00Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms
    • C07D409/02Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings
    • C07D409/06Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings linked by a carbon chain containing only aliphatic carbon atoms
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D409/00Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms
    • C07D409/02Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings
    • C07D409/12Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings linked by a chain containing hetero atoms as chain links
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D413/00Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
    • C07D413/02Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
    • C07D413/12Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings linked by a chain containing hetero atoms as chain links
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D413/00Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
    • C07D413/14Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing three or more hetero rings
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D417/00Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
    • C07D417/02Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings
    • C07D417/12Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D471/00Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
    • C07D471/02Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
    • C07D471/04Ortho-condensed systems

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • Medicinal Chemistry (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • General Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Engineering & Computer Science (AREA)
  • Dermatology (AREA)
  • Hematology (AREA)
  • Oncology (AREA)
  • Epidemiology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Saccharide Compounds (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
  • Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
  • Agricultural Chemicals And Associated Chemicals (AREA)
  • Pyridine Compounds (AREA)
  • Medicines Containing Material From Animals Or Micro-Organisms (AREA)

Abstract

Disclosed are compounds of Formula (I) and pharmaceutically acceptable salts and solvates thereof. Such compounds are MEK inhibitors and are useful in the treatment of proliferative diseases, such as cancer. Also disclosed are pharmaceutical compositions containing such compounds as well as methods of using the compounds and compositions of the invention in the treatment of cancer.
LU93078C 2005-10-07 2016-05-19 COMBIMETINIB, POSSIBLY IN ANY FORM PROTECTED BY THE BASIC PATENT, INCLUDING PHARMACEUTICALLY ACCEPTABLE SALTS AND SOLVATES, IN PARTICULAR COBIMETINIB HEMIFUMARATE LU93078I2 (en)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US72457805P 2005-10-07 2005-10-07
US80284006P 2006-05-23 2006-05-23
PCT/US2006/039126 WO2007044515A1 (en) 2005-10-07 2006-10-05 Azetidines as mek inhibitors for the treatment of proliferative diseases

Publications (1)

Publication Number Publication Date
LU93078I2 true LU93078I2 (en) 2016-07-19

Family

ID=37728416

Family Applications (1)

Application Number Title Priority Date Filing Date
LU93078C LU93078I2 (en) 2005-10-07 2016-05-19 COMBIMETINIB, POSSIBLY IN ANY FORM PROTECTED BY THE BASIC PATENT, INCLUDING PHARMACEUTICALLY ACCEPTABLE SALTS AND SOLVATES, IN PARTICULAR COBIMETINIB HEMIFUMARATE

Country Status (32)

Country Link
US (9) US7803839B2 (en)
EP (1) EP1934174B1 (en)
JP (8) JP5129143B2 (en)
KR (2) KR20130058072A (en)
CN (5) CN109053523B (en)
AT (1) ATE504565T1 (en)
AU (1) AU2006302415B2 (en)
BE (1) BE2016C029I2 (en)
BR (1) BRPI0617165B1 (en)
CA (3) CA3052368A1 (en)
CY (2) CY1111670T1 (en)
DE (1) DE602006021205D1 (en)
DK (1) DK1934174T3 (en)
EA (3) EA032466B1 (en)
ES (1) ES2365070T3 (en)
FR (1) FR16C0021I2 (en)
GE (1) GEP20125456B (en)
HR (1) HRP20110498T1 (en)
HU (1) HUS1600021I1 (en)
IL (5) IL189900A (en)
LT (1) LTC1934174I2 (en)
LU (1) LU93078I2 (en)
MY (1) MY162174A (en)
NL (1) NL300809I2 (en)
NO (4) NO347091B1 (en)
NZ (1) NZ567140A (en)
PL (1) PL1934174T3 (en)
PT (1) PT1934174E (en)
RS (1) RS51782B (en)
SI (1) SI1934174T1 (en)
WO (1) WO2007044515A1 (en)
ZA (1) ZA200802075B (en)

Families Citing this family (271)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
MX2007004781A (en) * 2004-10-20 2007-05-11 Applied Research Systems 3-arylamino pyridine derivatives.
HRP20110498T1 (en) * 2005-10-07 2011-08-31 Exelixis AZETIDINS AS MAK INHIBITORS FOR THE TREATMENT OF PROLIFERATIVE DISEASES
GB0601962D0 (en) 2006-01-31 2006-03-15 Ucb Sa Therapeutic agents
CN101528231A (en) 2006-08-16 2009-09-09 埃克塞利希斯股份有限公司 Use of PI3K and MEK modulators in the treatment of cancer
EP2089359A2 (en) 2006-10-31 2009-08-19 Takeda Pharmaceutical Company Limited Mapk/erk kinase inhibitors
WO2008076415A1 (en) 2006-12-14 2008-06-26 Exelixis, Inc. Methods of using mek inhibitors
WO2008124085A2 (en) * 2007-04-03 2008-10-16 Exelixis, Inc. Methods of using combinations of mek and jak-2 inhibitors
WO2008139287A1 (en) * 2007-05-10 2008-11-20 Pfizer Limited Azetidine derivatives and their use as prostaglandin e2 antagonists
NZ583318A (en) 2007-07-16 2012-07-27 Genentech Inc Humanized anti-cd79b antibodies and immunoconjugates and methods of use
DK2474557T3 (en) 2007-07-16 2014-11-10 Genentech Inc Anti-CD79b antibodies and immune conjugates and methods of use
GB0714384D0 (en) 2007-07-23 2007-09-05 Ucb Pharma Sa theraputic agents
WO2009093008A1 (en) 2008-01-21 2009-07-30 Ucb Pharma S.A. Thieno-pyridine derivatives as mek inhibitors
SG187517A1 (en) 2008-01-31 2013-02-28 Genentech Inc Anti-cd79b antibodies and immunoconjugates and methods of use
NZ602675A (en) 2008-03-18 2014-03-28 Genentech Inc Combinations of an anti-her2 antibody-drug conjugate and chemotherapeutic agents, and methods of use
GB0811304D0 (en) 2008-06-19 2008-07-30 Ucb Pharma Sa Therapeutic agents
RU2509078C2 (en) 2008-07-01 2014-03-10 Дженентек, Инк. Bicyclic heterocycles as mek kinase inhibitors
MX2010014565A (en) 2008-07-01 2011-03-04 Genentech Inc Isoindolone derivatives as mek kinase inhibitors and methods of use.
EP2370568B1 (en) 2008-12-10 2017-07-19 Dana-Farber Cancer Institute, Inc. Mek mutations conferring resistance to mek inhibitors
CN102369011A (en) 2009-03-12 2012-03-07 健泰科生物技术公司 Combinations of phosphoinositide 3-kinase inhibitor compounds and chemotherapeutic agents for the treatment of hematopoietic malignancies
CN102459272B (en) 2009-05-27 2014-08-06 健泰科生物技术公司 Bicyclic pyrimidine PI3K inhibitor compounds selective for P110 delta, and methods of use
ES2558742T3 (en) 2009-09-28 2016-02-08 F. Hoffmann-La Roche Ag Benzoxepine PI3K inhibitor compounds and methods of use
ES2570569T3 (en) 2009-09-28 2016-05-19 Hoffmann La Roche Benzoxazepine compounds as PI3K inhibitors and methods of use
KR101489045B1 (en) * 2009-10-12 2015-02-02 에프. 호프만-라 로슈 아게 Combinations of a pi3k inhibitor and a mek inhibitor
JP5466767B2 (en) * 2009-11-04 2014-04-09 ノバルティス アーゲー Heterocyclic sulfonamide derivatives useful as MEK inhibitors
US20110165155A1 (en) 2009-12-04 2011-07-07 Genentech, Inc. Methods of treating metastatic breast cancer with trastuzumab-mcc-dm1
EP2526102B1 (en) 2010-01-22 2017-03-08 Fundación Centro Nacional de Investigaciones Oncológicas Carlos III Inhibitors of PI3 kinase
MX2012009059A (en) 2010-02-22 2012-09-07 Hoffmann La Roche Pyrido[3,2-d]pyrimidine pi3k delta inhibitor compounds and methods of use.
EP3028699B1 (en) 2010-02-25 2018-03-21 Dana-Farber Cancer Institute, Inc. Braf mutations conferring resistance to braf inhibitors
CN103038364A (en) 2010-03-09 2013-04-10 达纳-法伯癌症研究所公司 Methods of diagnosing and treating cancer in patients having or developing resistance to a first cancer therapy
WO2011121317A1 (en) 2010-04-01 2011-10-06 Centro Nacional De Investigaciones Oncologicas (Cnio) Imidazo [2,1-b] [1,3,4] thiadiazoles as protein or lipid kinase inhibitors
JP6161537B2 (en) 2010-04-07 2017-07-12 エフ・ホフマン−ラ・ロシュ・アクチェンゲゼルシャフト Pyrazol-4-yl-heterocyclyl-carboxamide compounds and methods of use
DK2528625T3 (en) 2010-04-15 2013-10-14 Spirogen Sarl Pyrrolobenzodiazepines and their conjugates
KR101862327B1 (en) 2010-05-07 2018-05-29 질레드 코네티컷 인코포레이티드 Pyridone and aza-pyridone compounds and methods of use
JP5555378B2 (en) 2010-07-14 2014-07-23 エフ.ホフマン−ラ ロシュ アーゲー Purine compounds selective for PI3KP110 delta and methods of use thereof
CA2806670A1 (en) 2010-07-26 2012-02-09 Biomatrica, Inc. Compositions for stabilizing dna, rna and proteins in blood and other biological samples during shipping and storage at ambient temperatures
US9845489B2 (en) 2010-07-26 2017-12-19 Biomatrica, Inc. Compositions for stabilizing DNA, RNA and proteins in saliva and other biological samples during shipping and storage at ambient temperatures
CA2809836C (en) 2010-09-01 2019-01-15 Gilead Connecticut, Inc. Pyridinones/pyrazinones, method of making, and method of use thereof for the treatment of disorders mediated by bruton's tyrosine kinase
BR112013007499A2 (en) 2010-09-01 2016-07-12 Genentech Inc pyridazinones - rearing methods and uses
WO2012052745A1 (en) 2010-10-21 2012-04-26 Centro Nacional De Investigaciones Oncológicas (Cnio) Combinations of pi3k inhibitors with a second anti -tumor agent
US20140080810A1 (en) 2010-11-15 2014-03-20 Exelixis, Inc. Benzoxazepines as Inhibitors of PI3K/mTOR and Methods of Their Use and Manufacture
CN103313989B (en) 2010-12-16 2016-05-04 霍夫曼-拉罗奇有限公司 Tricyclic PI3K inhibitor compounds and methods of use
CA2825028A1 (en) 2011-02-09 2012-08-16 F. Hoffman-La Roche Ag Heterocyclic compounds as pi3 kinase inhibitors
WO2012126901A1 (en) 2011-03-21 2012-09-27 F. Hoffmann-La Roche Ag Benzoxazepin compounds selective for pi3k p110 delta and methods of use
CN102718750B (en) * 2011-03-31 2015-03-11 中国人民解放军军事医学科学院毒物药物研究所 Aminopyridine derivatives containing acridine ring and application thereof
TR201815685T4 (en) * 2011-04-01 2018-11-21 Genentech Inc Combinations of act and mec inhibitory compounds for the treatment of cancer.
KR102021157B1 (en) 2011-04-01 2019-09-11 제넨테크, 인크. Combinations of akt inhibitor compounds and abiraterone, and methods of use
AU2012257513B2 (en) 2011-05-19 2017-05-11 Fundación Del Sector Público Estatal Centro Nacional De Investigaciones Oncológicas Carlos III (F.S.P. CNIO) Macrocyclic compounds as protein kinase inhibitors
EP2524918A1 (en) 2011-05-19 2012-11-21 Centro Nacional de Investigaciones Oncológicas (CNIO) Imidazopyrazines derivates as kinase inhibitors
KR20140040728A (en) 2011-06-03 2014-04-03 에프. 호프만-라 로슈 아게 Methods of treating mesothelioma with a pi3k inhibitor compound
JP6238459B2 (en) 2011-08-01 2017-11-29 ジェネンテック, インコーポレイテッド Method for treating cancer using PD-1 axis binding antagonist and MEK inhibitor
JP6133291B2 (en) 2011-08-12 2017-05-24 エフ・ホフマン−ラ・ロシュ・アクチェンゲゼルシャフト Pyrazolo [3,4-c] pyridine compounds and methods of use
AR088061A1 (en) 2011-09-27 2014-05-07 Hoffmann La Roche COMPOUNDS OF PIRAZOL-4-IL-HETEROCICLIL-CARBOXAMIDE AND METHODS OF USE
JP6104257B2 (en) 2011-10-14 2017-03-29 メドイミューン・リミテッドMedImmune Limited Pyrrolobenzodiazepine and its conjugates
PE20142312A1 (en) * 2011-10-28 2015-01-25 Genentech Inc THERAPEUTIC COMBINATIONS AND METHODS TO TREAT MELANOMA
UA111756C2 (en) 2011-11-03 2016-06-10 Ф. Хоффманн-Ля Рош Аг HETEROARYLPYRIDONE AND AZAPIRIDONE COMPOUNDS AS BRUTON TYROSINKINASE INHIBITORS
RU2628616C2 (en) 2011-11-03 2017-08-21 Ф. Хоффманн-Ля Рош Аг Bicyclic piperazine compounds
MX2014005289A (en) 2011-11-03 2014-05-30 Hoffmann La Roche Alkylated piperazine compounds as inhibitors of btk activity.
WO2013067264A1 (en) 2011-11-03 2013-05-10 Genentech, Inc. 8-fluorophthalazin-1 (2h) - one compounds as inhibitors of btk activity
EP2592103A1 (en) 2011-11-08 2013-05-15 Adriacell S.p.A. Polymer aldehyde derivatives
JP2015501639A (en) 2011-11-23 2015-01-19 アイジェニカ バイオセラピューティクス インコーポレイテッド Anti-CD98 antibody and method of use thereof
WO2013082511A1 (en) 2011-12-02 2013-06-06 Genentech, Inc. Methods for overcoming tumor resistance to vegf antagonists
CN103204827B (en) 2012-01-17 2014-12-03 上海科州药物研发有限公司 Benzothiadiazole compounds as protein kinase inhibitors, and preparation method and application thereof
WO2013113102A1 (en) 2012-02-01 2013-08-08 The Governors Of The University Of Alberta USE OF PDGFR-α AS DIAGNOSTIC MARKER FOR PAPILLARY THYROID CANCER
US20150141470A1 (en) 2012-05-08 2015-05-21 The Broad Institute, Inc. Diagnostic and treatment methods in patients having or at risk of developing resistance to cancer therapy
WO2013182668A1 (en) 2012-06-08 2013-12-12 F. Hoffmann-La Roche Ag Mutant selectivity and combinations of a phosphoinositide 3 kinase inhibitor compound and chemotherapeutic agents for the treatment of cancer
BR112014029674A2 (en) 2012-06-27 2017-06-27 Hoffmann La Roche compound, pharmaceutical composition, method for treating a disease, use of a compound, kit for treating a pim kinase-mediated condition and invention
MX2015001407A (en) 2012-08-02 2015-05-08 Genentech Inc Anti-etbr antibodies and immunoconjugates.
CA2879665A1 (en) 2012-08-02 2014-02-06 Genentech, Inc. Anti-etbr antibodies and immunoconjugates
EP3626309B1 (en) * 2012-08-13 2023-03-08 The Rockefeller University Lxrbeta agonist for the treatment of cancer
DK2884979T3 (en) 2012-08-17 2019-09-02 Hoffmann La Roche Combination treatments for melanoma including administration of cobimetinib and vemurafenib
MX361157B (en) 2012-08-30 2018-11-28 Hoffmann La Roche Dioxino- and oxazin-[2,3-d]pyrimidine pi3k inhibitor compounds and methods of use.
DK2900657T3 (en) 2012-09-26 2020-05-04 Hoffmann La Roche Cyclic etherpyrazol-4-yl-heterocyclyl-carboxamide compounds and methods of use
WO2014059028A1 (en) 2012-10-09 2014-04-17 Igenica, Inc. Anti-c16orf54 antibodies and methods of use thereof
CN104837502B (en) 2012-10-12 2018-08-10 麦迪穆有限责任公司 Pyrrolobenzodiazepines and their conjugates
DK2906298T3 (en) 2012-10-12 2018-12-17 Adc Therapeutics Sa Pyrrolobenzodiazepine-antibody conjugates
MA38085B1 (en) 2012-10-12 2018-11-30 Exelixis Inc New process for the production of compounds for use in the treatment of cancer
US10751346B2 (en) 2012-10-12 2020-08-25 Medimmune Limited Pyrrolobenzodiazepine—anti-PSMA antibody conjugates
ES2649990T3 (en) 2012-10-12 2018-01-16 Medimmune Limited Anti-CD22-pyrrolobenzodiazepine antibody conjugates
EP2906250B1 (en) 2012-10-12 2018-05-30 ADC Therapeutics SA Pyrrolobenzodiazepine-anti-psma antibody conjugates
AU2013328625B2 (en) 2012-10-12 2016-12-15 Adc Therapeutics Sa Pyrrolobenzodiazepine-antibody conjugates
AU2013328674B2 (en) 2012-10-12 2017-06-22 Medimmune Limited Pyrrolobenzodiazepines and conjugates thereof
US10695433B2 (en) 2012-10-12 2020-06-30 Medimmune Limited Pyrrolobenzodiazepine-antibody conjugates
WO2014074785A1 (en) 2012-11-08 2014-05-15 Ludwig Institute For Cancer Research Ltd. Methods of predicting outcome and treating breast cancer
WO2014078669A1 (en) * 2012-11-15 2014-05-22 Duquesne University Of The Holy Ghost Carboxylic acid ester prodrug inhibitors of mek
TW201441193A (en) * 2012-12-06 2014-11-01 Kyowa Hakko Kirin Co Ltd Pyridone compound
US9725703B2 (en) 2012-12-20 2017-08-08 Biomatrica, Inc. Formulations and methods for stabilizing PCR reagents
CN105246894A (en) 2012-12-21 2016-01-13 斯皮罗根有限公司 Asymmetric pyrrolobenzodiazepine dimers for the treatment of proliferative and autoimmune diseases
CN105189507A (en) 2012-12-21 2015-12-23 斯皮罗根有限公司 Pyrrolobenzodiazepines and conjugates thereof
EP2958592A1 (en) 2013-02-22 2015-12-30 F. Hoffmann-La Roche AG Methods of treating cancer and preventing drug resistance
BR112015019909A2 (en) 2013-02-22 2017-08-29 Abbvie Stemcentrx Llc ANTIBODY-DRUG CONJUGATES, PHARMACEUTICAL COMPOSITION, THEIR USES, AND KIT
ES2703208T3 (en) 2013-02-27 2019-03-07 Daiichi Sankyo Co Ltd Method for predicting sensitivity to a compound that inhibits the MAPK signal transduction pathway
SG11201507214SA (en) 2013-03-13 2015-10-29 Medimmune Ltd Pyrrolobenzodiazepines and conjugates thereof
NZ710746A (en) 2013-03-13 2018-11-30 Medimmune Ltd Pyrrolobenzodiazepines and conjugates thereof
CA2905181C (en) 2013-03-13 2020-06-02 Medimmune Limited Pyrrolobenzodiazepines and conjugates thereof for providing targeted therapy
JP2016515132A (en) 2013-03-14 2016-05-26 ジェネンテック, インコーポレイテッド Combination and use of MEK inhibitor compounds with HER3 / EGFR inhibitor compounds
DK2968346T3 (en) 2013-03-15 2024-05-06 Cancer Research Tech Llc Methods and compositions for modulating the gamma-glutamyl cycle
EP2975936A4 (en) 2013-03-22 2017-03-15 University of Hawaii Novel stat3 inhibitors
SG11201509982UA (en) 2013-06-06 2016-04-28 Igenica Biotherapeutics Inc
CN105491883B (en) 2013-06-13 2018-11-02 生物马特里卡公司 Cell stabilization
RU2016101548A (en) 2013-07-03 2017-08-08 Ф. Хоффманн-Ля Рош Аг Compounds of amides of heteroarylpyridone and azapyridone
AU2014312215B2 (en) 2013-08-28 2020-02-27 Abbvie Stemcentrx Llc Site-specific antibody conjugation methods and compositions
US9532987B2 (en) * 2013-09-05 2017-01-03 Genentech, Inc. Use of a combination of a MEK inhibitor and an ERK inhibitor for treatment of hyperproliferative diseases
AU2014391422A1 (en) 2013-09-17 2015-12-17 Obi Pharma, Inc. Compositions of a carbohydrate vaccine for inducing immune responses and uses thereof in cancer treatment
GB201317982D0 (en) 2013-10-11 2013-11-27 Spirogen Sarl Pyrrolobenzodiazepines and conjugates thereof
EP3054986B1 (en) 2013-10-11 2019-03-20 Medimmune Limited Pyrrolobenzodiazepine-antibody conjugates
EP3054985B1 (en) 2013-10-11 2018-12-26 Medimmune Limited Pyrrolobenzodiazepine-antibody conjugates
US10010624B2 (en) 2013-10-11 2018-07-03 Medimmune Limited Pyrrolobenzodiazepine-antibody conjugates
WO2015082583A1 (en) 2013-12-05 2015-06-11 F. Hoffmann-La Roche Ag Heteroaryl pyridone and aza-pyridone compounds with electrophilic functionality
US10214584B2 (en) 2014-01-15 2019-02-26 Order-Made Medical Research Inc. Therapeutic pharmaceutical composition employing anti-SLC6A6 antibody
CN104788365B (en) * 2014-01-16 2018-08-10 上海艾力斯医药科技有限公司 Pyrazinamide derivative, preparation method and application
JP6554480B2 (en) 2014-03-18 2019-07-31 エフ・ホフマン−ラ・ロシュ・アクチェンゲゼルシャフト Oxepan-2-yl-pyrazol-4-yl-heterocyclyl-carboxamide compounds and methods of use
GB201406767D0 (en) 2014-04-15 2014-05-28 Cancer Rec Tech Ltd Humanized anti-Tn-MUC1 antibodies anf their conjugates
CA2946112C (en) 2014-04-18 2020-11-24 The Governors Of The University Of Alberta Targeted therapy to restore radioactive iodine transport in thyroid cancer
JP2017513901A (en) 2014-04-25 2017-06-01 ジェネンテック, インコーポレイテッド Method of treating early stage breast cancer with trastuzumab-MCC-DM1 and pertuzumab
US11293915B2 (en) 2014-05-08 2022-04-05 Cornell University Bio-adhesive gels and methods of use
WO2015182734A1 (en) * 2014-05-30 2015-12-03 協和発酵キリン株式会社 Nitrogen-containing heterocyclic compound
CN106572650B (en) 2014-06-10 2021-08-31 生物马特里卡公司 Stabilizes thrombocytes at ambient temperature
SG11201700074YA (en) 2014-07-15 2017-02-27 Genentech Inc Compositions for treating cancer using pd-1 axis binding antagonists and mek inhibitors
JP6531166B2 (en) 2014-09-10 2019-06-12 メドイミューン・リミテッドMedImmune Limited Pyrrolobenzodiazepine and its conjugate
LT3191135T (en) 2014-09-12 2020-11-25 Genentech, Inc. ANTI-HER2 ANTIBODIES AND IMMUNOCONJUGATES
MX2017003123A (en) 2014-09-12 2017-05-12 Genentech Inc Cysteine engineered antibodies and conjugates.
GB201416112D0 (en) 2014-09-12 2014-10-29 Medimmune Ltd Pyrrolobenzodiazepines and conjugates thereof
US20160074527A1 (en) 2014-09-17 2016-03-17 Genentech, Inc. Pyrrolobenzodiazepines and antibody disulfide conjugates thereof
HK1243629A1 (en) 2014-09-17 2018-07-20 基因泰克公司 Immunoconjugates comprising anti-her2 antibodies and pyrrolobenzodiazepines
JP6507234B2 (en) 2014-10-02 2019-04-24 エフ.ホフマン−ラ ロシュ アーゲーF. Hoffmann−La Roche Aktiengesellschaft Pyrazole carboxamide compounds for use in the treatment of disorders mediated by bruton tyrosine kinase (BTK)
WO2016061253A1 (en) 2014-10-14 2016-04-21 Exelixis, Inc. Drug combination to treat melanoma
AU2015352545B2 (en) 2014-11-25 2020-10-15 Adc Therapeutics Sa Pyrrolobenzodiazepine-antibody conjugates
PL3333191T3 (en) 2014-12-11 2021-05-04 Pierre Fabre Médicament Anti-c10orf54 antibodies and uses thereof
WO2016095089A1 (en) * 2014-12-15 2016-06-23 Merck Sharp & Dohme Corp. Erk inhibitors
WO2016095088A1 (en) 2014-12-15 2016-06-23 Merck Sharp & Dohme Corp. Erk inhibitors
KR102785474B1 (en) 2014-12-18 2025-03-26 에프. 호프만-라 로슈 아게 TETRAHYDRO-PYRIDO[3,4-b]INDOLE ESTROGEN RECEPTOR MODULATORS AND USES THEREOF
WO2016164916A1 (en) 2015-04-10 2016-10-13 Thomas Jefferson University Methods and compositions for treating cancers and enhancing therapeutic immunity by selectively reducing immunomodulatory m2 monocytes
GB201506411D0 (en) 2015-04-15 2015-05-27 Bergenbio As Humanized anti-axl antibodies
GB201506402D0 (en) 2015-04-15 2015-05-27 Berkel Patricius H C Van And Howard Philip W Site-specific antibody-drug conjugates
GB201506389D0 (en) 2015-04-15 2015-05-27 Berkel Patricius H C Van And Howard Philip W Site-specific antibody-drug conjugates
US11406715B2 (en) 2015-05-30 2022-08-09 Genentech, Inc. Methods of treating HER2-positive metastatic breast cancer
CN108064246A (en) 2015-06-15 2018-05-22 基因泰克公司 Antibody and immune conjugate
AR105483A1 (en) * 2015-06-30 2017-10-11 Exelixis Inc CRYSTAL FUMARATE SALT OF (S) - [3,4-DIFLUORO-2- (2-FLUORO-4-IODOPHENYLAMINE) PHENYL] [3-HIDROXI-3- (PIPERIDIN-2-IL) AZETIDIN-1-IL] - METANONE
CA2987912C (en) 2015-06-30 2023-01-24 Genentech, Inc. Immediate-release tablets containing a drug and processes for forming the tablets
EP4212536B1 (en) 2015-07-02 2025-02-19 F. Hoffmann-La Roche AG Benzoxazepin oxazolidinone compounds and methods of use
WO2017001658A1 (en) 2015-07-02 2017-01-05 F. Hoffmann-La Roche Ag Benzoxazepin oxazolidinone compounds and methods of use
US20190008859A1 (en) 2015-08-21 2019-01-10 Acerta Pharma B.V. Therapeutic Combinations of a MEK Inhibitor and a BTK Inhibitor
KR20180050339A (en) 2015-09-04 2018-05-14 오비아이 파머 인코퍼레이티드 Glycan arrays and how to use them
AU2016349279A1 (en) 2015-11-03 2018-05-10 Board Of Regents, The University Of Texas System Combination of Bcl-2 inhibitor and MEK inhibitor for the treatment of cancer
WO2017087280A1 (en) 2015-11-16 2017-05-26 Genentech, Inc. Methods of treating her2-positive cancer
CN121154828A (en) 2015-11-19 2025-12-19 豪夫迈·罗氏有限公司 Methods of treating cancer using B-RAF inhibitors and immune checkpoint inhibitors
SG11201804776SA (en) 2015-12-08 2018-07-30 Biomatrica Inc Reduction of erythrocyte sedimentation rate
CN105330643B (en) * 2015-12-09 2017-12-05 苏州明锐医药科技有限公司 Card is than the preparation method for Buddhist nun
GB201601431D0 (en) 2016-01-26 2016-03-09 Medimmune Ltd Pyrrolobenzodiazepines
GB201602356D0 (en) 2016-02-10 2016-03-23 Medimmune Ltd Pyrrolobenzodiazepine Conjugates
GB201602359D0 (en) 2016-02-10 2016-03-23 Medimmune Ltd Pyrrolobenzodiazepine Conjugates
EP4049660B1 (en) 2016-02-29 2025-02-19 F. Hoffmann-La Roche AG Dosage form compositions comprising an inhibitor of bruton's tyrosine kinase
EP3424505A4 (en) 2016-03-04 2019-10-16 Taiho Pharmaceutical Co., Ltd. PREPARATION AND COMPOSITION FOR TREATING MALIGNANT TUMORS
US11883404B2 (en) 2016-03-04 2024-01-30 Taiho Pharmaceuticals Co., Ltd. Preparation and composition for treatment of malignant tumors
US10980894B2 (en) 2016-03-29 2021-04-20 Obi Pharma, Inc. Antibodies, pharmaceutical compositions and methods
AU2017239637A1 (en) 2016-03-29 2018-11-15 Obi Pharma, Inc. Antibodies, pharmaceutical compositions and methods
WO2017180581A1 (en) 2016-04-15 2017-10-19 Genentech, Inc. Diagnostic and therapeutic methods for cancer
CN109379889A (en) 2016-04-22 2019-02-22 台湾浩鼎生技股份有限公司 Cancer immunotherapy by immune activation or immunomodulation via antigens of the GLOBO series
GB201607478D0 (en) 2016-04-29 2016-06-15 Medimmune Ltd Pyrrolobenzodiazepine Conjugates
CN106045969B (en) * 2016-05-27 2019-04-12 湖南欧亚药业有限公司 A kind of synthetic method of the card than replacing Buddhist nun
JP7018026B2 (en) 2016-06-16 2022-02-09 エフ・ホフマン-ラ・ロシュ・アクチェンゲゼルシャフト Heteroarylestrogen receptor modulator and its use
US20170362228A1 (en) 2016-06-16 2017-12-21 Genentech, Inc. TETRAHYDRO-PYRIDO[3,4-b]INDOLE ESTROGEN RECEPTOR MODULATORS AND USES THEREOF
KR20230117482A (en) 2016-07-27 2023-08-08 오비아이 파머 인코퍼레이티드 Immunogenic/therapeutic glycan compositions and uses thereof
CN106220607B (en) * 2016-07-27 2018-09-18 成都百事兴科技实业有限公司 A kind of synthetic method of S-3- (piperidin-2-yl)-aza-cyclobutane -3-alcohol
WO2018023121A1 (en) 2016-07-29 2018-02-01 Obi Pharma, Inc. Human antibodies, pharmaceutical compositions and methods
AU2017311585A1 (en) 2016-08-12 2019-02-28 Genentech, Inc. Combination therapy with a MEK inhibitor, a PD-1 axis inhibitor, and a VEGF inhibitor
AU2017335839A1 (en) 2016-09-29 2019-04-18 Genentech, Inc. Combination therapy with a MEK inhibitor, a PD-1 axis inhibitor, and a taxane
GB201617466D0 (en) 2016-10-14 2016-11-30 Medimmune Ltd Pyrrolobenzodiazepine conjugates
TWI822055B (en) 2016-11-21 2023-11-11 台灣浩鼎生技股份有限公司 Conjugated biological molecules, pharmaceutical compositions and methods
GB201702031D0 (en) 2017-02-08 2017-03-22 Medlmmune Ltd Pyrrolobenzodiazepine-antibody conjugates
MX375569B (en) 2017-02-08 2025-03-04 Adc Therapeutics Sa PYRROLOBENZODIAZEPINES AND ANTIBODIES CONJUGATES
SI3579883T1 (en) 2017-02-08 2021-12-31 Adc Therapeutics Sa Pyrrolobenzodiazepine-antibody conjugates
CN106866624B (en) * 2017-02-27 2017-12-26 济宁医学院 It is a kind of to block than the chemical synthesis process for Buddhist nun
EP3606536A4 (en) 2017-04-04 2020-12-16 University of Miami BIOMARKERS FOR PROSTATE CANCER AND TREATMENT THEREOF
PT3612537T (en) 2017-04-18 2022-08-29 Medimmune Ltd Pyrrolobenzodiazepine conjugates
ES2977788T3 (en) 2017-04-20 2024-08-30 Adc Therapeutics Sa Combination therapy with an anti-AXL antibody-drug conjugate
AU2018253950A1 (en) 2017-04-20 2019-09-19 Adc Therapeutics Sa Combination therapy with an anti-CD25 antibody-drug conjugate
BR112019026498A2 (en) 2017-06-14 2020-07-14 Adc Therapeutics Sa dosing regimens for administration of an anti-cd25 adc
MX2019015042A (en) 2017-06-14 2020-08-06 Adc Therapeutics Sa DOSAGE REGIME.
DK3668874T3 (en) 2017-08-18 2022-02-14 Medimmune Ltd Pyrrolobenzodiazepine conjugates
AU2018329925B2 (en) 2017-09-08 2025-05-29 F. Hoffmann-La Roche Ag Diagnostic and therapeutic methods for cancer
EP3752200A1 (en) 2018-02-13 2020-12-23 Vib Vzw Targeting minimal residual disease in cancer with rxr antagonists
GB201803342D0 (en) 2018-03-01 2018-04-18 Medimmune Ltd Methods
SG11202008435SA (en) 2018-03-19 2020-10-29 Taiho Pharmaceutical Co Ltd Pharmaceutical composition including sodium alkyl sulfate
WO2019183320A1 (en) 2018-03-21 2019-09-26 Colorado State University Research Foundation Cancer vaccine compositions and methods of use thereof
EP3757676A4 (en) 2018-03-26 2021-04-07 FUJIFILM Corporation COMPOSITION OF PHOTOSENSITIVE RESIN, ASSOCIATED PRODUCTION PROCESS, RESERVE FILM, PATTERN FORMATION PROCESS AND PRODUCTION PROCESS OF AN ELECTRONIC DEVICE
GB201806022D0 (en) 2018-04-12 2018-05-30 Medimmune Ltd Pyrrolobenzodiazepines and conjugates thereof
CA3098103A1 (en) 2018-05-23 2019-11-28 Adc Therapeutics Sa Molecular adjuvant
WO2020006176A1 (en) 2018-06-27 2020-01-02 Obi Pharma, Inc. Glycosynthase variants for glycoprotein engineering and methods of use
GB201811364D0 (en) 2018-07-11 2018-08-29 Adc Therapeutics Sa Combination therapy
KR102767692B1 (en) 2018-07-20 2025-02-17 피에르 파브르 메디카먼트 VISTA's receptor
CN112638392B (en) 2018-08-31 2024-09-10 Adc治疗有限公司 Combination therapy
US20210348238A1 (en) 2018-10-16 2021-11-11 Novartis Ag Tumor mutation burden alone or in combination with immune markers as biomarkers for predicting response to targeted therapy
MA55143A (en) * 2018-11-20 2021-09-29 H Lee Moffitt Cancer Center & Res Institute Inc ARYL-ANILINE AND HETEROARYL-ANILINE COMPOUNDS FOR THE TREATMENT OF SKIN CANCERS
AU2019383311B2 (en) * 2018-11-20 2024-12-05 Nflection Therapeutics, Inc. Cyanoaryl-aniline compounds for treatment of dermal disorders
US12466818B2 (en) 2018-11-20 2025-11-11 Nflection Therapeutics, Inc. Thienyl-aniline compounds for treatment of dermal disorders
CN113473986B (en) 2018-11-20 2024-10-11 恩福莱克逊治疗有限公司 Naphthyridoneaniline compounds for the treatment of skin disorders
WO2020109251A1 (en) 2018-11-29 2020-06-04 Adc Therapeutics Sa Dosage regime
US20220347309A1 (en) 2018-12-19 2022-11-03 Adc Therapeutics Sa Pyrrolobenzodiazepine resistance
GB201820725D0 (en) 2018-12-19 2019-01-30 Adc Therapeutics Sarl Pyrrolobenzodiazepine resistance
JPWO2020130125A1 (en) 2018-12-21 2021-11-04 第一三共株式会社 Combination of antibody-drug conjugate and kinase inhibitor
KR102890251B1 (en) 2019-03-15 2025-11-25 메드임뮨 리미티드 Azetidobenzodiazepine dimers and conjugates comprising the same for use in the treatment of cancer
WO2020187674A1 (en) 2019-03-15 2020-09-24 Sandoz Ag Crystalline (s)-[3,4-difluoro-2-(2-fluoro-4-iodophenylamino)phenyl][3-hydroxy-3-(piperidin-2-yl)azetidin-1-yl]methanone hemisuccinate
US20220143049A1 (en) 2019-03-21 2022-05-12 Onxeo A dbait molecule in combination with kinase inhibitor for the treatment of cancer
HUE060364T2 (en) 2019-03-29 2023-02-28 Medimmune Ltd Compounds and conjugates thereof
TWI735210B (en) 2019-04-26 2021-08-01 中國醫藥大學 Use of adam9 inhibitor as immune modulator
GB201908128D0 (en) 2019-06-07 2019-07-24 Adc Therapeutics Sa Pyrrolobenzodiazepine-antibody conjugates
CA3142664A1 (en) 2019-06-10 2020-12-17 Adc Therapeutics Sa Combination therapy comprising an anti-cd25 antibody drug conjugate and a further agent
JP7740994B2 (en) 2019-06-10 2025-09-17 アーデーセー セラピューティクス ソシエテ アノニム Combination Therapies Comprising Anti-CD19 Antibody Drug Conjugates and PI3K Inhibitors or Second-Line Agents
LT4004002T (en) 2019-07-22 2024-10-25 Lupin Limited MACROCYCLIC COMPOUNDS AS STING AGONISTS AND METHODS AND METHODS OF USE THEREOF
GB201912059D0 (en) 2019-08-22 2019-10-09 Bergenbio As Combaination therapy of a patient subgroup
US20240123081A1 (en) 2019-10-25 2024-04-18 Medimmune, Llc Branched moiety for use in conjugates
EP4054579A1 (en) 2019-11-08 2022-09-14 Institut National de la Santé et de la Recherche Médicale (INSERM) Methods for the treatment of cancers that have acquired resistance to kinase inhibitors
GB201917254D0 (en) 2019-11-27 2020-01-08 Adc Therapeutics Sa Combination therapy
HUE067466T2 (en) 2019-12-13 2024-10-28 Inspirna Inc Metal salts and uses thereof
CN111170990B (en) * 2020-01-16 2021-01-05 广州科锐特生物科技有限公司 Preparation method of 3-piperidine-2-yl-azetidine-3-ol derivative
WO2021148500A1 (en) 2020-01-22 2021-07-29 Medimmune Limited Compounds and conjugates thereof
WO2021148581A1 (en) 2020-01-22 2021-07-29 Onxeo Novel dbait molecule and its use
TW202140076A (en) 2020-01-22 2021-11-01 英商梅迪繆思有限公司 Compounds and conjugates thereof
GB202004189D0 (en) 2020-03-23 2020-05-06 Bergenbio As Combination therapy
JP7805285B2 (en) 2020-04-10 2026-01-23 大鵬薬品工業株式会社 Cancer treatment method using 3,5-disubstituted benzenealkynyl compound and MEK inhibitor
IL319200A (en) 2020-04-16 2025-04-01 Regeneron Pharma Antibody-drug conjugates prepared using diels-alder conjugation methods
GB202006072D0 (en) 2020-04-24 2020-06-10 Bergenbio Asa Method of selecting patients for treatment with cmbination therapy
EP3915576A1 (en) 2020-05-28 2021-12-01 Fundació Privada Institut d'Investigació Oncològica de Vall-Hebron Chimeric antigen receptors specific for p95her2 and uses thereof
EP3939999A1 (en) 2020-07-14 2022-01-19 Fundación del Sector Público Estatal Centro Nacional de Investigaciones Oncológicas Carlos III (F.S.P. CNIO) Interleukin 11 receptor alpha subunit (il11ra) neutralizing antibodies and uses thereof
GB202011993D0 (en) 2020-07-31 2020-09-16 Adc Therapeutics Sa ANTI-IL 13Ra2 antibodies
GB202012161D0 (en) 2020-08-05 2020-09-16 Adc Therapeutics Sa Combination therapy
JP2023537626A (en) 2020-08-14 2023-09-04 グアンジョウ・ルペン・ファーマシューティカル・カンパニー・リミテッド Dosage composition comprising an inhibitor of BTK and its variants
GB202015226D0 (en) 2020-09-25 2020-11-11 Adc Therapeutics S A Pyrrol obenzodiazepine-antibody conugates and uses thereof
GB202015916D0 (en) 2020-10-07 2020-11-18 Adc Therapeutics Sa Combination therapy
US20230372528A1 (en) 2020-10-16 2023-11-23 University Of Georgia Research Foundation, Inc. Glycoconjugates
GB202102396D0 (en) 2021-02-19 2021-04-07 Adc Therapeutics Sa Molecular adjuvant
JP2024509269A (en) 2021-03-09 2024-02-29 ジェネンテック, インコーポレイテッド Bervarafenib for use in the treatment of brain cancer
CN117321418A (en) 2021-03-18 2023-12-29 诺华股份有限公司 Cancer biomarkers and how to use them
EP4319749A1 (en) 2021-04-06 2024-02-14 Genentech, Inc. Combination therapy with belvarafenib and cobimetinib or with belvarafenib, cobimetinib, and atezolizumab
EP4346826A4 (en) 2021-05-27 2025-04-30 Mirati Therapeutics, Inc. Combination therapies
GB202107706D0 (en) 2021-05-28 2021-07-14 Adc Therapeutics S A Combination therapy
GB202107713D0 (en) 2021-05-28 2021-07-14 Medimmune Ltd Combination therapy
GB202107709D0 (en) 2021-05-28 2021-07-14 Adc Therapeutics S A Combination therapy
BR112023025916A2 (en) 2021-06-09 2024-02-27 Chugai Pharmaceutical Co Ltd COMBINATION OF A BRAF INHIBITOR AND A MEK INHIBITOR, USE OF A COMBINATION, METHOD FOR THE TREATMENT OR PROPHYLAXIS OF CANCER, PHARMACEUTICAL COMPOSITIONS AND INVENTION
WO2023274974A1 (en) 2021-06-29 2023-01-05 Adc Therapeutics Sa Combination therapy using antibody-drug conjugates
WO2023057545A1 (en) 2021-10-06 2023-04-13 Microquin Ltd. Substituted chalcones
AU2022383040A1 (en) 2021-11-04 2024-03-07 F. Hoffmann-La Roche Ag Novel use of quinazolinone compound for the treatment of cancer
KR20240125577A (en) 2021-11-23 2024-08-19 엔플렉션 테라퓨틱스, 인코포레이티드 Formulation of pyrrolopyridine-aniline compounds
WO2023111213A1 (en) 2021-12-16 2023-06-22 Rdp Pharma Ag Cell penetrating polypeptides (cpps) and their use in human therapy
TW202342018A (en) 2022-03-04 2023-11-01 美商奇奈特生物製藥公司 Inhibitors of mek kinase
US11780800B1 (en) 2022-03-17 2023-10-10 Springworks Therapeutics, Inc. Fluorinated phenylamino compounds and pharmaceutical compositions
EP4253418A1 (en) 2022-03-29 2023-10-04 Fundació Privada Institut d'Investigació Oncològica de Vall-Hebron Immune cells expressing chimeric antigen receptors and bispecific antibodies and uses thereof
GB202209285D0 (en) 2022-06-24 2022-08-10 Bergenbio Asa Dosage regimen for AXL inhibitor
WO2024033381A1 (en) 2022-08-10 2024-02-15 Vib Vzw Inhibition of tcf4/itf2 in the treatment of cancer
CN120265291A (en) 2022-11-18 2025-07-04 豪夫迈·罗氏有限公司 New uses and preparations of quinazolinone compounds
EP4406973A1 (en) 2023-01-27 2024-07-31 Fundació Privada Institut de Recerca de la SIDA-Caixa Antibodies and uses thereof for the treatment of infections caused by enveloped viruses
JPWO2024209717A1 (en) 2023-04-06 2024-10-10
AU2024265078A1 (en) 2023-05-04 2025-12-11 Revolution Medicines, Inc. Combination therapy for a ras related disease or disorder
WO2025029650A1 (en) 2023-07-28 2025-02-06 Li Xiyan Nutritionally modified diets comprising aminoacids for use in treating a disease
IL326136A (en) 2023-08-07 2026-03-01 Revolution Medicines Inc Rmc-6291 for use in the treatment of ras protein-related disease or disorder
WO2025073765A1 (en) 2023-10-03 2025-04-10 Institut National de la Santé et de la Recherche Médicale Methods of prognosis and treatment of patients suffering from melanoma
US20250154171A1 (en) 2023-10-12 2025-05-15 Revolution Medicines, Inc. Ras inhibitors
WO2025171296A1 (en) 2024-02-09 2025-08-14 Revolution Medicines, Inc. Ras inhibitors
WO2025240847A1 (en) 2024-05-17 2025-11-20 Revolution Medicines, Inc. Ras inhibitors
US20250375445A1 (en) 2024-06-07 2025-12-11 Revolution Medicines, Inc. Methods of treating a ras protein-related disease or disorder
WO2025265060A1 (en) 2024-06-21 2025-12-26 Revolution Medicines, Inc. Therapeutic compositions and methods for managing treatment-related effects
WO2026006747A1 (en) 2024-06-28 2026-01-02 Revolution Medicines, Inc. Ras inhibitors
WO2026015801A1 (en) 2024-07-12 2026-01-15 Revolution Medicines, Inc. Methods of treating a ras related disease or disorder
WO2026015825A1 (en) 2024-07-12 2026-01-15 Revolution Medicines, Inc. Use of ras inhibitor for treating pancreatic cancer
WO2026015790A1 (en) 2024-07-12 2026-01-15 Revolution Medicines, Inc. Methods of treating a ras related disease or disorder
WO2026015796A1 (en) 2024-07-12 2026-01-15 Revolution Medicines, Inc. Methods of treating a ras related disease or disorder
WO2026019990A1 (en) 2024-07-18 2026-01-22 Genentech, Inc. Methods of treating cancer with anti-ccr8/anti-cd3 bispecific antibodies
WO2026024841A1 (en) 2024-07-24 2026-01-29 Astellas Us Llc Bispecific antibodies that bind cd3 and muc1 and methods of use thereof
WO2026050446A1 (en) 2024-08-29 2026-03-05 Revolution Medicines, Inc. Ras inhibitors
WO2026072904A2 (en) 2024-09-26 2026-04-02 Revolution Medicines, Inc. Compositions and methods for treating lung cancer

Family Cites Families (62)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4510139A (en) * 1984-01-06 1985-04-09 Sterling Drug Inc. Substituted aminobenzamides and their use as agents which inhibit lipoxygenase activity
US5155110A (en) 1987-10-27 1992-10-13 Warner-Lambert Company Fenamic acid hydroxamate derivatives having cyclooxygenase and 5-lipoxygenase inhibition
JPH03192592A (en) 1989-12-21 1991-08-22 Matsushita Electric Ind Co Ltd Magnetic tape recording/playback device
CA2186947A1 (en) * 1994-04-01 1995-10-12 Kazuo Ueda Oxime derivative and bactericide containing the same as active ingredients
WO1997012613A1 (en) 1995-10-05 1997-04-10 Warner-Lambert Company Method for treating and preventing inflammation and atherosclerosis
WO1998037881A1 (en) 1997-02-28 1998-09-03 Warner Lambert Company Method of treating or preventing septic shock by administering a mek inhibitor
CA2290509A1 (en) * 1997-07-01 1999-01-14 Warner-Lambert Company 2-(4-bromo or 4-iodo phenylamino) benzoic acid derivatives and their use as mek inhibitors
NZ501276A (en) 1997-07-01 2000-10-27 Warner Lambert Co 4-bromo or 4-iodo phenylamino benzhydroxamic acid derivatives and their use as MEK inhibitors in treating proliferative disorders
US6974878B2 (en) * 2001-03-21 2005-12-13 Symyx Technologies, Inc. Catalyst ligands, catalytic metal complexes and processes using same
AU2180500A (en) 1998-12-15 2000-07-03 Warner-Lambert Company Use of a mek inhibitor for preventing transplant rejection
AU776788C (en) * 1998-12-16 2005-10-27 Warner-Lambert Company Treatment of arthritis with MEK inhibitors
PL348326A1 (en) 1998-12-22 2002-05-20 Warner Lambert Co Combination chemotherapy
KR20000047461A (en) 1998-12-29 2000-07-25 성재갑 Thrombin inhibitors
AU2203800A (en) 1999-01-07 2000-07-24 Warner-Lambert Company Antiviral method using mek inhibitors
JP2002534380A (en) 1999-01-07 2002-10-15 ワーナー−ランバート・カンパニー Treatment of asthma with MEK inhibitors
CA2348236A1 (en) 1999-01-13 2000-07-20 Stephen Douglas Barrett 4-arylamino, 4-aryloxy, and 4-arylthio diarylamines and derivatives thereof as selective mek inhibitors
CA2349832A1 (en) 1999-01-13 2000-07-20 Warner-Lambert Company Benzenesulfonamide derivatives and their use as mek inhibitors
CA2355470C (en) 1999-01-13 2008-09-30 Warner-Lambert Company Benzoheterocycles and their use as mek inhibitors
HUP0105092A3 (en) 1999-01-13 2003-12-29 Warner Lambert Co 1-heterocycle substituted diarylamines and medicaments containing them
EP1150950A2 (en) 1999-01-13 2001-11-07 Warner-Lambert Company Anthranilic acid derivatives
EP1202732A2 (en) 1999-07-16 2002-05-08 Warner-Lambert Company Llc Method for treating chronic pain using mek inhibitors
JP2003504400A (en) 1999-07-16 2003-02-04 ワーナー−ランバート・カンパニー Method for treating chronic pain using MEK inhibitor
JP2003504401A (en) 1999-07-16 2003-02-04 ワーナー−ランバート・カンパニー Method for treating chronic pain using MEK inhibitor
CA2377092A1 (en) 1999-07-16 2001-01-25 Warner-Lambert Company Method for treating chronic pain using mek inhibitors
DE60040676D1 (en) 1999-09-17 2008-12-11 Millennium Pharm Inc BENZAMIDES AND SIMILAR INHIBITORS OF FACTOR Xa
BR0109188A (en) 2000-03-15 2003-03-18 Warner Lambert Co Substituted 5-Amide Diarylamines as Mex Inhibitors
AR033517A1 (en) 2000-04-08 2003-12-26 Astrazeneca Ab PIPERIDINE DERIVATIVES, PROCESS FOR THE PREPARATION AND USE OF THESE DERIVATIVES IN THE MANUFACTURE OF MEDICINES
DZ3401A1 (en) 2000-07-19 2002-01-24 Warner Lambert Co OXYGEN ESTERS OF 4-IODOPHENYLAMINO BENZHYDROXAMIC ACIDS
IL149462A0 (en) 2001-05-09 2002-11-10 Warner Lambert Co Method of treating or inhibiting neutrophil chemotaxis by administering a mek inhibitor
DE10141266A1 (en) * 2001-08-21 2003-03-06 Syntec Ges Fuer Chemie Und Tec Electroluminescent derivatives of 2,5-diamino-terephthalic acid and their use in organic light-emitting diodes
JP2003192592A (en) 2001-10-17 2003-07-09 Sankyo Co Ltd Pharmaceutical composition
CN1568184A (en) 2001-10-31 2005-01-19 辉瑞产品公司 Use of nicotinic acetylcholine receptor agonists in the treatment of restless legs syndrome
DOP2003000556A (en) 2002-01-23 2003-10-31 Warner Lambert Co ESTERES HYDROXAMATE ACID N- (4-PHENYL-REPLACED) -ANTRANILICO.
EP1467968A1 (en) 2002-01-23 2004-10-20 Warner-Lambert Company LLC N-(4-substituted phenyl)-anthranilic acid hydroxamate esters
EP1482944A4 (en) * 2002-03-13 2006-04-19 Array Biopharma Inc N3 alkylated benzimidazole derivatives as mek inhibitors
US7235537B2 (en) * 2002-03-13 2007-06-26 Array Biopharma, Inc. N3 alkylated benzimidazole derivatives as MEK inhibitors
SG2013013339A (en) * 2002-03-13 2014-12-30 Array Biopharma Inc N3 alkylated benzimidazole derivatives as mek inhibitors
EP1515727A4 (en) 2002-06-11 2009-04-08 Merck & Co Inc INHIBITORS OF P38 KINASE (HALO-BENZO CARBONYL) HETEROBICYCLIC
GB0214268D0 (en) * 2002-06-20 2002-07-31 Celltech R&D Ltd Chemical compounds
US20050004186A1 (en) 2002-12-20 2005-01-06 Pfizer Inc MEK inhibiting compounds
CA2517517C (en) * 2003-03-03 2012-12-18 Array Biopharma, Inc. P38 inhibitors and methods of use thereof
TW200505834A (en) 2003-03-18 2005-02-16 Sankyo Co Sulfamide derivative and the pharmaceutical composition thereof
JP2005162727A (en) 2003-03-18 2005-06-23 Sankyo Co Ltd Sulfamide derivative and medicinal preparation thereof
GB0308185D0 (en) 2003-04-09 2003-05-14 Smithkline Beecham Corp Novel compounds
EP1641804A1 (en) * 2003-06-20 2006-04-05 Celltech R & D Limited Thienopyridone derivatives as kinase inhibitors
WO2005000818A1 (en) 2003-06-27 2005-01-06 Warner-Lambert Company Llc 5-substituted-4-`(substituted phenyl)!amino!-2-pyridone deviatives for use as mek inhibitors
WO2005007616A1 (en) * 2003-07-23 2005-01-27 Warner-Lambert Company Llc Diphenylamino ketone derivatives as mek inhibitors
US20050049276A1 (en) * 2003-07-23 2005-03-03 Warner-Lambert Company, Llc Imidazopyridines and triazolopyridines
CA2532067C (en) * 2003-07-24 2010-12-21 Stephen Douglas Barrett N-methyle-substituted benzamidazoles
US7538120B2 (en) * 2003-09-03 2009-05-26 Array Biopharma Inc. Method of treating inflammatory diseases
US7144907B2 (en) * 2003-09-03 2006-12-05 Array Biopharma Inc. Heterocyclic inhibitors of MEK and methods of use thereof
US8084645B2 (en) * 2003-09-19 2011-12-27 Chugai Seiyaku Kabushiki Kaisha 4-phenylamino-benzaldoxime derivatives and uses thereof as mitogen-activated protein kinase kinase (MEK) inhibitors
CA2546353A1 (en) * 2003-11-19 2005-06-09 Array Biopharma Inc. Bicyclic inhibitors of mek and methods of use thereof
US7517994B2 (en) * 2003-11-19 2009-04-14 Array Biopharma Inc. Heterocyclic inhibitors of MEK and methods of use thereof
CA2547804A1 (en) * 2003-12-08 2005-06-30 F. Hoffmann-La Roche Ag Novel thiazole derivatives
MY144232A (en) 2004-07-26 2011-08-15 Chugai Pharmaceutical Co Ltd 5-substituted-2-phenylamino benzamides as mek inhibitors
AR050084A1 (en) 2004-07-27 2006-09-27 Novartis Ag BENCIMIDAZOLONE DERIVATIVES AS HSP90 INHIBITORS
MX2007004781A (en) 2004-10-20 2007-05-11 Applied Research Systems 3-arylamino pyridine derivatives.
WO2006061712A2 (en) 2004-12-10 2006-06-15 Pfizer Inc. Use of mek inhibitors in treating abnormal cell growth
US7547782B2 (en) 2005-09-30 2009-06-16 Bristol-Myers Squibb Company Met kinase inhibitors
HRP20110498T1 (en) * 2005-10-07 2011-08-31 Exelixis AZETIDINS AS MAK INHIBITORS FOR THE TREATMENT OF PROLIFERATIVE DISEASES
CN101528231A (en) * 2006-08-16 2009-09-09 埃克塞利希斯股份有限公司 Use of PI3K and MEK modulators in the treatment of cancer

Also Published As

Publication number Publication date
US7803839B2 (en) 2010-09-28
EA025871B9 (en) 2017-08-31
ATE504565T1 (en) 2011-04-15
JP2017101071A (en) 2017-06-08
IL189900A (en) 2014-06-30
CY2016015I1 (en) 2016-10-05
JP2020189882A (en) 2020-11-26
CY1111670T1 (en) 2015-10-07
LTC1934174I2 (en) 2018-01-10
CN104892582A (en) 2015-09-09
JP5856211B2 (en) 2016-02-09
JP2014111659A (en) 2014-06-19
HK1119698A1 (en) 2009-03-13
NZ567140A (en) 2011-09-30
FR16C0021I2 (en) 2017-04-14
CN109053523A (en) 2018-12-21
CY2016015I2 (en) 2016-10-05
US7915250B2 (en) 2011-03-29
KR20080050601A (en) 2008-06-09
EA201691142A1 (en) 2017-02-28
ES2365070T3 (en) 2011-09-21
BRPI0617165B1 (en) 2023-10-03
IL251185A0 (en) 2017-05-29
NO20200035A1 (en) 2008-06-17
NO2023022I1 (en) 2023-05-11
US11597699B2 (en) 2023-03-07
US20250100966A1 (en) 2025-03-27
KR101341792B1 (en) 2013-12-23
HUS1600021I1 (en) 2016-06-28
JP2015232045A (en) 2015-12-24
US20150141399A1 (en) 2015-05-21
AU2006302415A1 (en) 2007-04-19
CN103524392A (en) 2014-01-22
CN109053523B (en) 2022-03-25
DK1934174T3 (en) 2011-08-01
US20110263558A1 (en) 2011-10-27
RS51782B (en) 2011-12-31
WO2007044515A1 (en) 2007-04-19
US20190144382A1 (en) 2019-05-16
JP5678019B2 (en) 2015-02-25
LTPA2016016I1 (en) 2016-06-10
CN110668988A (en) 2020-01-10
GEP20125456B (en) 2012-03-26
IL260127A (en) 2018-07-31
CA2927656C (en) 2019-09-24
IL260127B (en) 2022-04-01
EA201400111A1 (en) 2014-09-30
EP1934174A1 (en) 2008-06-25
US20170166523A9 (en) 2017-06-15
CN101365676B (en) 2013-09-11
JP2019089841A (en) 2019-06-13
CA3052368A1 (en) 2007-04-19
EA025871B1 (en) 2017-02-28
CA2927656A1 (en) 2007-04-19
JP2018058907A (en) 2018-04-12
HRP20110498T1 (en) 2011-08-31
JP5129143B2 (en) 2013-01-23
AU2006302415B2 (en) 2012-09-13
EA032466B1 (en) 2019-05-31
JP2009511490A (en) 2009-03-19
SI1934174T1 (en) 2011-08-31
NO344876B1 (en) 2020-06-08
US20140275527A1 (en) 2014-09-18
IL233053A0 (en) 2014-07-31
NO20082088L (en) 2008-06-17
IL229136A (en) 2015-11-30
CN103524392B (en) 2018-06-01
ZA200802075B (en) 2009-08-26
HK1214595A1 (en) 2016-07-29
US20090156576A1 (en) 2009-06-18
NO347091B1 (en) 2023-05-15
DE602006021205D1 (en) 2011-05-19
BE2016C029I2 (en) 2026-01-14
NO2020031I1 (en) 2020-09-04
CA2622755A1 (en) 2007-04-19
US20200283383A1 (en) 2020-09-10
IL229136A0 (en) 2013-12-31
CN104892582B (en) 2019-09-27
US20200031770A1 (en) 2020-01-30
NL300809I2 (en) 2016-10-19
CN101365676A (en) 2009-02-11
JP2013014601A (en) 2013-01-24
CA2622755C (en) 2017-01-31
KR20130058072A (en) 2013-06-03
MY162174A (en) 2017-05-31
PT1934174E (en) 2011-07-14
EA019983B1 (en) 2014-07-30
BRPI0617165A2 (en) 2015-01-06
PL1934174T3 (en) 2011-09-30
EP1934174B1 (en) 2011-04-06
US20100249096A1 (en) 2010-09-30
US8362002B2 (en) 2013-01-29
EA200801041A1 (en) 2009-02-27
FR16C0021I1 (en) 2016-06-24
IL189900A0 (en) 2008-08-07

Similar Documents

Publication Publication Date Title
LU93078I2 (en) COMBIMETINIB, POSSIBLY IN ANY FORM PROTECTED BY THE BASIC PATENT, INCLUDING PHARMACEUTICALLY ACCEPTABLE SALTS AND SOLVATES, IN PARTICULAR COBIMETINIB HEMIFUMARATE
UA109417C2 (en) Substituted piperidines, which improve activity of p53, and use thereof
TW200613243A (en) Novel compounds
IL189666A0 (en) Pyridinaminosulfonyl substituted benzamides as inhibitors of cytochrome p450 3a4 (cyp3a4)
MX2010003868A (en) Chiral cis-imidazolines.
PT1940839E (en) Pyridopyrimidinone inhibitors of pi3kalpha
CY1112019T1 (en) NIACINI RECEPTORS RACE, COMPOSITIONS CONTAINING COMPOSITIONAL COMPOUNDS AND METHODS OF TREATMENT
MY149512A (en) Pyrazolylaminopyridine derivatives useful as kinase inhibitors
EA201001196A1 (en) 4-PYRIDINONE COMPOUNDS AND THEIR APPLICATION FOR CANCER TREATMENT
ATE532789T1 (en) DIHYDROTHIENOPYRIMIDINES AS ACT PROTEIN KINASE INHIBITORS
TW200508207A (en) New benzimidazole derivatives
DE60313350D1 (en) PYRIMIDIN-2,4-DION DERIVATIVES AS MATRIX METALLOPROTEINASE INHIBITORS
TW200626553A (en) Novel compounds
TW200639156A (en) New compounds
UA96742C2 (en) Mek inhibitors and use thereof
EA201990219A3 (en) MEK INHIBITORS AND WAYS OF THEIR APPLICATION
DK1551850T3 (en) 2 "-oxo-voruscharin and its derivatives
UA95250C2 (en) Pyridinaminosulfonyl substituted benzamides as inhibitors of cytochrome p450 3a4 (cyp4503a4)